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Clinical Use of Cinacalcet in MEN1 Hyperparathyroidism
Background. Management of multiple-endocrine neoplasia type 1- (MEN1-) associated hyperparathyroidism is associated with high recurrence rates and high surgical morbidity due to multiple neck explorations. Cinacalcet, a calcimimetic agent licensed for the treatment of secondary hyperparathyroidism a...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2877200/ https://www.ncbi.nlm.nih.gov/pubmed/20585352 http://dx.doi.org/10.1155/2010/906163 |
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author | Moyes, V. J. Monson, J. P. Chew, S. L. Akker, S. A. |
author_facet | Moyes, V. J. Monson, J. P. Chew, S. L. Akker, S. A. |
author_sort | Moyes, V. J. |
collection | PubMed |
description | Background. Management of multiple-endocrine neoplasia type 1- (MEN1-) associated hyperparathyroidism is associated with high recurrence rates and high surgical morbidity due to multiple neck explorations. Cinacalcet, a calcimimetic agent licensed for the treatment of secondary hyperparathyroidism and parathyroid carcinoma, may provide a medical alternative for the management of these complex patients. Methods. A prospective audit was performed of eight patients; three males and five females, aged 20–38 at diagnosis. Two patients commenced cinacalcet as primary treatment and six had previous surgery. Six patients had complications of hyperparathyroidism: renal calculi, renal dysfunction, and reduced bone mineral density. All were commenced on cinacalcet 30 mg bd for MEN1 associated hyperparathyroidism; doses were subsequently reduced to 30 mg od in four patients. Results. Significant reductions were observed in serum calcium and PTH measurements. Serum calcium reduced by a median of 0.35 mmol/L (P = .012 Wilcoxon Signed Rank). Serum PTH levels decreased by a median of 5.05 pmol/L (P = .012). There was no change in urine calcium. Duration ranged from 10–35 months with maintenance of control. Cinacalcet was well tolerated by six patients; one experienced nausea and one experienced diarrhoea. Conclusion. Cinacalcet is an effective and well-tolerated medical treatment for the management of complex primary hyperparathyroidism. |
format | Text |
id | pubmed-2877200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-28772002010-06-28 Clinical Use of Cinacalcet in MEN1 Hyperparathyroidism Moyes, V. J. Monson, J. P. Chew, S. L. Akker, S. A. Int J Endocrinol Clinical Study Background. Management of multiple-endocrine neoplasia type 1- (MEN1-) associated hyperparathyroidism is associated with high recurrence rates and high surgical morbidity due to multiple neck explorations. Cinacalcet, a calcimimetic agent licensed for the treatment of secondary hyperparathyroidism and parathyroid carcinoma, may provide a medical alternative for the management of these complex patients. Methods. A prospective audit was performed of eight patients; three males and five females, aged 20–38 at diagnosis. Two patients commenced cinacalcet as primary treatment and six had previous surgery. Six patients had complications of hyperparathyroidism: renal calculi, renal dysfunction, and reduced bone mineral density. All were commenced on cinacalcet 30 mg bd for MEN1 associated hyperparathyroidism; doses were subsequently reduced to 30 mg od in four patients. Results. Significant reductions were observed in serum calcium and PTH measurements. Serum calcium reduced by a median of 0.35 mmol/L (P = .012 Wilcoxon Signed Rank). Serum PTH levels decreased by a median of 5.05 pmol/L (P = .012). There was no change in urine calcium. Duration ranged from 10–35 months with maintenance of control. Cinacalcet was well tolerated by six patients; one experienced nausea and one experienced diarrhoea. Conclusion. Cinacalcet is an effective and well-tolerated medical treatment for the management of complex primary hyperparathyroidism. Hindawi Publishing Corporation 2010 2010-05-26 /pmc/articles/PMC2877200/ /pubmed/20585352 http://dx.doi.org/10.1155/2010/906163 Text en Copyright © 2010 V. J. Moyes et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Study Moyes, V. J. Monson, J. P. Chew, S. L. Akker, S. A. Clinical Use of Cinacalcet in MEN1 Hyperparathyroidism |
title | Clinical Use of Cinacalcet in MEN1 Hyperparathyroidism |
title_full | Clinical Use of Cinacalcet in MEN1 Hyperparathyroidism |
title_fullStr | Clinical Use of Cinacalcet in MEN1 Hyperparathyroidism |
title_full_unstemmed | Clinical Use of Cinacalcet in MEN1 Hyperparathyroidism |
title_short | Clinical Use of Cinacalcet in MEN1 Hyperparathyroidism |
title_sort | clinical use of cinacalcet in men1 hyperparathyroidism |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2877200/ https://www.ncbi.nlm.nih.gov/pubmed/20585352 http://dx.doi.org/10.1155/2010/906163 |
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